Clinical and genetic characteristics of new allele variants of the Mowat–Wilson syndrome caused by ZEB2 gene mutations by I. A. Akimova, T. V. Markova, F. A. Konovalov, A. V. Antonets, E. L. Dadali

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Impaired nutrient absorption, reduced bone mass and alterations in the gut microbiome contribute to postnatal growth retardation in a mouse model of MWS by Yangyang Ge, Lingya Liu, Lihua Wu, Xiaofan Liu, Yingao Hao, Shixu Wang, Yi Xiong, Zi Yang, Zhen Zhang, Qi Li, Bo Li, Jianxin Wu, Guangxu Ren, Qian Jiang

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miR-200b regulates cellular senescence and inflammatory responses by targeting ZEB2 in pulmonary emphysema by Zhiming Shen, Wenting Xuan, Huanhuan Wang, Fei Sun, Chengxin Zhang, Qian Gong, Shenglin Ge

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MOWAT-WILSON SYNDROME: DEEP PHENOTYPING AND MOLECULAR CHARACTERISATION OF TWELVE NEW INDIVIDUALS by Umut Altunoğlu, Nilay Güneş, Gözde Tutku Turgut, Tuğba Kalaycı, Ayça Dilruba Aslanger, Murat Derbent, Serpil Eraslan, Birsen Karaman, Zehra Oya Uyguner, Beyhan Tüysüz, Yasemin Alanay, Hülya Kayserili Karabey

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Heterogeneity of CD8αα intraepithelial lymphocytes is transcriptionally conserved between TCRαβ and TCRγδ cell lineages by Kaito A. Hioki, Kaito A. Hioki, Kaito A. Hioki, Xueting Liang, Xueting Liang, Adam C. Lynch, Adam C. Lynch, Adam C. Lynch, Ravi Ranjan, Elena L. Pobezinskaya, Leonid A. Pobezinsky, Leonid A. Pobezinsky

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Mowat-Wilson syndrome: literature review and case series by M. Yu. Bobylova, V. S. Kakaulina, M. O. Abramov, K. Yu. Mukhin

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